1) TEBAC
三乙基苄基氯化铵(TEBAC)
2) triethylbenzylammonium chloride
氯化三乙基苄基铵
1.
The title compound C24H22N2O2 has been synthesized by the reaction of N-arylidenenaphthalen-2-amine with 5,5-dimethyl-1,3-cyclohexadione water catalyzed by triethylbenzylammonium chlorideTEBAC.
标题化合物C24H22N2O2是由N-(4-羟基苯亚甲基)喹啉-5-胺和5,5-二甲基-1,3-环己二酮在氯化三乙基苄基铵(TEBAC)催化下以水作溶剂反应而得。
2.
The title compound C_(25)H_(22)ClNO has been synthesized by the reaction of N-arylidenenaphthalen-2-amine with 5,5-dimethyl-1,3-cyclohexadione in water catalyzed by triethylbenzylammonium chloride(TEBAC).
以N-(4-氯苯亚甲基)-2-萘胺和5,5-二甲基-1,3-环己二酮为原料,水作溶剂,在氯化三乙基苄基铵(TEBAC)催化下反应,得到标题化合物C25H22Cl2NO。
3) benzyl triethylammonium chloride
苄基三乙基氯化铵
1.
Inhibitory kinetic spectrophotometric determination of trace nickel in Ni(Ⅱ)-KBrO_3-methyl violet system with benzyl triethylammonium chloride as enhanced sensitivity agent;
以苄基三乙基氯化铵为增敏剂镍-溴酸钾-甲基紫体系阻抑动力学光度法测定痕量镍
2.
The method is based on the catalytic effect of iron(Ⅲ) on oxidation of bromocresol green by hydrogen peroxide(H_2O_2) using cationic surfactant of benzyl triethylammonium chloride(BTEAC) as sensitizer.
在增敏剂苄基三乙基氯化铵存在下,Fe(Ⅲ)对H2O2氧化溴甲酚绿具有催化作用,据此建立了一种测定痕量Fe(Ⅲ)的新方法。
4) benzyl triethyl ammonium chloride
苄基三乙基氯化铵
1.
The reactions were carried out in presence of benzyl triethyl ammonium chloride(BTEAC),and through ring-opening,rearrangement and hydration successively.
在相转移助剂苄基三乙基氯化铵(BTEAC)存在下,以氢型丝光沸石(HM)为催化剂,原料α-蒎烯经开环、重排及水合反应一步法合成了α-松油醇。
2.
In this paper,1,3- propanediol is synthesized using anhydrous sodium acetate,3- bromo- 1- chloropropane,anhydrous methanol,benzyl triethyl ammonium chloride and anion exchange resin etc.
文章以无水乙酸钠、3-溴-1-氯丙烷、苄基三乙基氯化铵、无水甲醇、717#离子交换树脂等为原料合成1,3-丙二醇,并对合成的产物用红外光谱、氢核磁共振波谱进行分析检测。
5) triethylbenzylammonium chloride
三乙基苄基氯化铵
1.
A series of 1-aryl-1,2-dihydrobenzo[f]quinolin-3(4H)-one derivatives were synthesized by a three-component one-pot reaction of benzaldehyde,naphthalene-2-amine and meldrum’s acid at refluxing temperature catalyzed by triethylbenzylammonium chloride in water.
以芳醛、2-萘胺和Meldrum酸为原料,以水为溶剂,在回流条件下以三乙基苄基氯化铵为催化剂通过三组分一锅反应,合成了一系列的1-芳基苯并[f]喹啉衍生物。
补充资料：苄基三乙基氯化铵
分子式：C13H22ClN
分子量：227.28
CAS号：56-37-1
性质：熔点185℃（分解）。
制备方法：将氯化苄、三乙胺、丙酮加入反应锅，在63-64℃回流8小时。缓缓降至15℃，过滤，滤饼用丙酮洗涤，干燥，得TEBA。收率68.9%。
用途：相转移催化剂。
分子量：227.28
CAS号：56-37-1
性质：熔点185℃（分解）。
制备方法：将氯化苄、三乙胺、丙酮加入反应锅，在63-64℃回流8小时。缓缓降至15℃，过滤，滤饼用丙酮洗涤，干燥，得TEBA。收率68.9%。
用途：相转移催化剂。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条